Реакция #214062

ord-c861772bef124816842f6f9cad1722f4

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe organic phase was separated off
  2. 2
    Сушкаdried over sodium sulphate
  3. 3
    Концентрированиеconcentrated
  4. 4
    workup.DISTILLATIONby distilling off the solvent in vacuo
  5. 5
    ДругоеThe base thus obtained
  6. 6
    workup.DISTILLATIONthe isopropanol was then distilled off
  7. 7
    workup.ADDITIONafter adding 100 ml of water
  8. 8
    workup.STIRRINGthe mixture was stirred at room temperature for a further 15 hours
  9. 9
    ДругоеThe organic phase was then separated off
  10. 10
    Промывкаwashed twice with 50 ml of water each time
  11. 11
    Сушкаdried over sodium sulphate
  12. 12
    Концентрированиеconcentrated
  13. 13
    ДругоеThe oil which remained was boiled up in 100 ml of petroleum ether, whereupon crystallization

Методика

18.8 g (0.04 mol) of 1-(4-chlorophenoxy)-1-(imidazol-1-yl)-3,3-dimethyl-4-chloro-butan-2-one naphthalene-1,5-disulphonate were suspended in 100 ml of methylene chloride, and 100 ml of sodium bicarbonate solution were added. The organic phase was separated off, dried over sodium sulphate and concentrated by distilling off the solvent in vacuo. The base thus obtained was taken up in 100 ml of isopropanol, and 2 g (0.05 mol) of sodium borohydride were added in portions at 5° to 10° C. The mixture was stirred at room temperature for 15 hours and the isopropanol was then distilled off. The residue was taken up in 100 ml of methylene chloride and, after adding 100 ml of water, the mixture was stirred at room temperature for a further 15 hours. The organic phase was then separated off, washed twice with 50 ml of water each time, dried over sodium sulphate and concentrated. The oil which remained was boiled up in 100 ml of petroleum ether, whereupon crystallization occurred. 9.8 g (75% of theory) of 1-(4-chlorophenoxy)-1-(imidazol-1-yl)-3,3-dimethyl-4-chloro-butan-2-ol of melting point 120°-125° C. were obtained. ##STR15##

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04254132uspto-grants-1981_03